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Molecular Medicine Peer-reviewed scientific journal

Molecular Medicine

ОРИГИНАЛЬНЫЕ ИССЛЕДОВАНИЯ

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

FAST MONITORING OF LONG-RANGE ORDER IN THE ENSEMBLE OF COLLAGEN DOMAINS IN THE ACHILLES TENDONS AND HUMAN KNEES IN VIVO

The dynamics of the collagen domain structure in the Achilles tendons and knees when they are stretched. Research method. A new non-invasive gravitational mass spectroscopy (GMS) method for operational (1...20 s) long-range order (LRO) monitoring in human tend…

10.29296/24999490-2019-03-10Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

COMPARATIVE CHARACTERISTICS OF THE SUSCEPTIBILITY OF KUPFFER CELLS AND MACROPHAGES OF BONE-BACKGROUND ORIGIN TO ACTIVATION FACTORS

Introduction. In mammals, there are several populations of macrophages, developing from bone marrow progenitors and resident macrophages, developing from the embryonic precursors of the yolk. One of the reasons for the coexistence of several populations of mac…

10.29296/24999490-2019-03-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

OPTIMIZATION OF THE METHOD OF THE MULTI-TARGET SINGLE-BASE ELONGATION FOR THE DETECTION OF SOMATIC MUTATIONS IN MALIGNANCIES

Background. Genotyping of the tumor samples is necessary for a personalized approach in the treatment of patients with malignancies. The identification of somatic mutations in EGFR and KRAS genes can help to predict the course of the disease and to individuali…

10.29296/24999490-2019-02-06Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

ACTIVATING POINT MUTATION OF BRCA1/2 GENES IN AZERBAIJAN POPULATION

Introduction. Breast cancer is the leading cancer type among woman of Azerbaijan population. Hereditary mutations of the BRCA1/2 genes are considered as high risk for appeared breast and ovarian cancers. In Azerbaijan BRCA1/2-related breast and ovarian cancer …

10.29296/24999490-2019-02-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

STUDY OF EXPRESSION OF MMP-1 GENE IN LOCALIZED SСLERODERMIA

The aim of the study was to investigate the expression of the MMP-1 gene in patients with a diagnosis of localized scleroderma. Methods. The study included 12 patients with an established diagnosis of localized scleroderma. The material of the study consisted …

10.29296/24999490-2019-02-04Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

THE SOME PECULIARITIES OF CAPSULAR FORMATION AFTER IMPLANTATION OF SILICONE WITH ADSORBED MULTIPOTENT MESENCHYMAL STROMAL CELLS

Introduction. The widespread cellular technologies will sooner or later lead inevitably to the introduction of multipotent mesenchymal stromal cells (MMSC) or their exosomes to patients who have implanted artificial materials in their organism. The engraftment…

10.29296/24999490-2019-02-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

MOLECULAR MECHANISMS OF RETARDATION OF SKIN AGING UNDER INFLUENCE 0F HUMAN PLACENTA HYDROLYSATE

Introduction. Application of placenta hydrolysate in cosmetology opens a new page in anti-aging therapy. Numerous studies have confirmed the antioxidant, anti-inflammatory, anti-pigmental properties of placenta hydrolysate preparations, as well as activation o…

10.29296/24999490-2019-02-07Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

THE STUDY OF THE ACUTE TOXICITY OF NEW RADIOPHARMACEUTICALS 99mTc-1-thio-D-glucose IN THE EXPERIMENT

The aim of the study. To investigate the overall acute toxicity of a new radiopharmaceutical in laboratory animals under the selected experimental conditions. Materials and methods. The study was performed on 80 white outbred rats (weight of males 220–260 g, t…

10.29296/24999490-2019-01-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

ANTIBODIES TO DESAMINATED GLYADIN PEPTIDES, TISSUE TRANSGLUTAMINASE AND ENDOMYSIUM IN HLA-DQ 2/8 GENOTYPE CARRIERS

Introduction. The laboratory diagnosis of celiac disease is based on the detection of antibodies against deamidated gliadin peptides (anti-DGP), autoantibodies to tissue transglutaminase (anti-tTG) and endomysium (AEA), as well as genotyping of HLA-DQ2/8 loci.…

10.29296/24999490-2019-01-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

COMPLEX F8 GENE REARRANGEMENTS

Introduction. Hemophilia A is a frequent X-linked recessive disorder associated with the absence or functional defect of blood clotting factor VIII. Вoth point mutations and large structural rearrangements – deletions, duplications, and inversions were describ…

10.29296/24999490-2019-01-07Details ↗
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